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Pirogoff Foot Size 24 Left

by Roadrunnerfoot Engineering srl

Ref 1.009.01.24.LModel SIZE 22,23,24,25,26,27,28,29 SIDE RIGHT/LEFT

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8055748721.009.01GM Basic UDI-DIDate30 Jun 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Pirogoff Foot
Model / Reference
SIZE 22, 23, 24, 25, 26, 27, 28, 29 SIDE RIGHT/LEFT, 1.009.01.24.L
Primary DI / UDI-DI
08055748721535
Basic UDI-DI
8055748721.009.01GM
EMDN Code
Y062499 Lower extremity prostheses - other
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008242

Other devices from Roadrunnerfoot Engineering srl

See all devices from Roadrunnerfoot Engineering srl →

Properties

Other properties (13)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No